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FDA 510(k)

CORNING BLOOD COLLECTION CAPILLARY TUBES

K-Number: K850806 · 1985-03-25

Decision Date1985-03-25
Product CodeGIO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CORNING BLOOD COLLECTION CAPILLARY TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Corning Medical & Scientific. It received FDA 510(k) clearance on 1985-03-25 under 510(k) number K850806. The device is classified under product code GIO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORNING BLOOD COLLECTION CAPILLARY TUBES?

CORNING BLOOD COLLECTION CAPILLARY TUBES is a medical device that received FDA 510(k) clearance on 1985-03-25. The listed applicant is Corning Medical & Scientific. The 510(k) number is K850806.

When did CORNING BLOOD COLLECTION CAPILLARY TUBES receive FDA 510(k) clearance?

CORNING BLOOD COLLECTION CAPILLARY TUBES received FDA 510(k) clearance on 1985-03-25, under 510(k) number K850806.

Who is the listed applicant for CORNING BLOOD COLLECTION CAPILLARY TUBES?

The FDA 510(k) record lists Corning Medical & Scientific as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORNING BLOOD COLLECTION CAPILLARY TUBES?

The FDA product code for CORNING BLOOD COLLECTION CAPILLARY TUBES is GIO.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Corning Medical & Scientific as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 111 devices →

Related Devices (Code: GIO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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